A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv38n223



Internal ID22803006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6376901..6385800hg38UCSC Ensembl
chr1:6436961..6445860hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg388900
hg198900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6320354, nsv6323530, nsv6334621
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv38n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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